Mobi-C Plug & Fit US

GUDID 03662663059176

Reinforced Rigid Distraction Forceps

LDR Spine Usa, Inc.

Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps Bone distraction forceps

Primary Device ID	03662663059176
NIH Device Record Key	93e56902-6302-45a7-8188-6fb646371d01
Commercial Distribution Status	In Commercial Distribution
Brand Name	Mobi-C Plug & Fit US
Version Model Number	MB9174R
Company DUNS	615789729
Company Name	LDR Spine Usa, Inc.
Device Count	1
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	03662663059176 [Primary]

FDA Product Code

GEN	Forceps, General & Plastic Surgery